National Pharmaceutical

Regulatory Agency,

MOH

Malaysian Organisation of

Pharmaceutical Industries

Organised by:

Presenter: ❖ Certificates endorsed by the National

Pharmaceutical Regulatory Agency,

Ministry of Health, Malaysia will be

awarded to participants upon successful

completion of each module.

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wwoorrkk ppllaaccee..

Who Should Attend Key Personnel in any Aspect of GMP & Quality Management, Managers, Engineers, Executives, Quality Practitioners and any member of a pharmaceutical and related industry, those from Research and Development, Quality and Production will find this program relevant and beneficial to their job function.

Trainers This course has been developed by SeerPharma and trainers are provided by, SeerPharma (Singapore) Pte Ltd. All SeerPharma trainers hold higher education degrees with a minimum of a Bachelor’s degree and have a number of years of industry experience in Quality Management or Production Management roles in major and multinational companies. They have experience in all international regulatory standards including FDA, EU, PIC/S, TGA and ISO. The trainer for each module will have specific expertise in that subject matter. SeerPharma is Australia’s and Asia Pacific’s premier training & consulting group offering integrated consulting, training and technical services to Australia and the Asia Pacific region to meet all international regulatory standards.

Training Grant

is available under HRDF SBL Scheme

For further details please visit www.mopi.org.my

YEAR 2018

Endorsed by:

Module 1 – International Good Manufacturing Practices, Quality Management Systems and GMP for Pharmaceutical Operations (23 – 25 January 2018) – 3 day Course

Aim: To provide an introduction to the regulations and Codes of Practice that governs the manufacture of therapeutic goods both nationally and internationally. To develop a broad understanding of the scope of Good Manufacturing Practices and Quality Management Systems applicable to drugs, devices and biologics and to provide a detailed analysis of the GMP requirements for manufacturing pharmaceuticals. Day 1 AM ►QA Principles & International GMPs, updates of ASEAN Harmonisation focusing on GMP PM ►Quality Management, Quality Assurance & Quality Control Day2 AM ►Key Quality Assurance Systems and GMP Responsibilities for Managers & Supervisors PM ►GMP Principles for Manufacturing Operations Day 3 AM ►GMP Principles for Packaging Operations includes control of printed packaging materials, line clearance and reconciliation of materials/products

AM ►GMP Principles for Warehousing (related to manufacturing) PM ►Equipment Management

Module 2 – Validation Principles and Practices (5 - 7 February 2018) – 3 day Course

Aim: This subject aims to introduce students to the validation principles covered in PIC/S, ICH, EU & FDA cGMPs and to extend the principles to practical outcomes.

Day 1 AM ►Validation Principles & International Regulations PM ►Validation Master Plans and Validation Documents PM ►Equipment Qualification and Commissioning Day 2 AM ►Introduction to Process Validation and Cleaning Validation PM ►Compiling URS against FDS documents PM ►Preparing DQ, IQ, OQ and PQ protocols Day 3 AM ►Protocol Execution AM ►Deviation Management PM ►Final Summary Report

Module 3 – Contamination Control (26 - 28 March 2018) – 3 day Course

Aim: To develop a broad understanding of the types and sources of contamination; and to analyze and assess the major risks to pharmaceuticals and the practical control methods which are used to minimize and correct contamination problems.

Day 1 AM ►Introduction to Contamination Control and why it is critical to product quality PM ►Microbiological Aspects of Manufacturing including routes of contamination. Identify the key controls within a manufacturing facility Day 2 AM ►Cleaning and Sanitation PM ►HVAC and Controlled Environments – control & qualification Day 3 AM ►Environmental Monitoring Programs PM ►Control of Water Systems

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FUNDAMENTAL COURSE OUTLINE

Behavourial GMP/Good Documentation Practices/Data Integrity (12 – 14 March 2018) – 3 day Course

Aim: To provide an introduction on the concepts of behavioural GMP and how they relate to human errors and incidents as well as develop methodologies for root cause analysis and failure investigation. This course helps quality managers and supervisors understand and identify personnel’s mentality and common behaviours and cultural changes to minimise human errors.

Day 1 Behavioural GMP AM/PM ► Knowledge and Understanding GMP concepts, compliance and improvement ►Discipline Skills – sources of human error and strategies to reduce human error in manufacturing

Day 2 Good Documentation Practices To understand the importance of creating documents and the need to maintain records in the industry to ensure compliance as well as traceability for processes and to prevent error. To understand the need for Good Documentation Practices to be applied throughout the manufacturing and supply chain. AM/PM ► Reasons and requirements for GMP documents and records ►Importance of document controls

►Current requirements for electronic records and signatories ►Handling of product complaints, recalls and CAPA

Day 3 Data Integrity

Data Integrity has become widely discussed as a global concern for the pharmaceutical industry. This section provides an introduction to develop a broad understanding of the scope of Data Integrity and how key principles may be applied in order to provide strategic elements necessary to ensure reliability and integrity of information and data throughout all aspects of a product’s lifecycle. AM/PM ► The definition of Data Integrity within a Quality Management System

►Regulatory framework for Data Integrity and Document Control Practices ►Behavioural GMP and development of a quality culture to enable Data Integrity compliance

With NEW CONTENT

Recommended for: All Personnel

Recommended for: All Personnel

Recommended for: QA, Engineers Production

Recommended for: QA and Production

Module 6 Good Distribution Practices (GDP) for the Regulated Industry (27 – 29 August 2018) – 3 day Course Aim: To provide an introduction to the requirements of Good Distribution Practices (GDPs) for the therapeutic and medical device industries, also provide a better understanding of the concepts of validation and management for the handling, storage and distribution of pharmaceutical products.

Day 1 AM ►Relationship and integration with GMP PM ►Understanding the manufacturer’s requirements Day 2 AM ►Risk Management and continuous improvement in distribution PM ►Understanding GDPs for therapeutic products and Devices PM ►Understanding GDPs for medical devices Day 3 AM ►Cold Chain Management – regulatory updates for the cold chain investigation, current and future, maintenance, handling and packaging of cold chain products PM ►Validation of the supply chain

PM ►Introduction to the principles of warehouse design for product preservation

Module 5 – Compliance with GMP for the Pharmaceutical Engineer (23 – 25 July 2018) – 3 day Course Aim: To provide an introduction to the requirements of Good Manufacturing Practices for supporting design of facilities, equipment and processes in the pharmaceutical and related industries, and to develop a broad understanding of the scope of Good Engineering Practices and Good Manufacturing Practices.

Day 1 AM ►Facility Layout and Design Principles PM ►Design and Construction of Critical Utilities: inc. Water, Gases and Steam Day 2 AM ►Water Systems: Design, Control & Validation PM ►HVAC Design, Control & Validation Day 3 AM ►Qualification of Processing Equipment PM ►Planned Preventative Maintenance and Calibration

Module 7 – Good Aseptic Practices & Sterile Products (24 – 26 September 2018) – 3 day Course Aim: This subject is designed to facilitate the development of knowledge and practical skills in the assessment of special risks associated with the manufacture of sterile pharmaceuticals and to develop and evaluate strategies and plans that will ensure acceptable sterility assurance levels.

Day 1 AM ►Assess the regulatory requirements for aseptic manufacturing processes in order to provide recommendations for their application to ensure compliance PM ►Evaluate the processing and compliance risks associated with aseptic processing and terminal sterilization Day 2 AM ►Critically evaluate strategies for bioburden control PM ►Evaluate the available processes for sterilisation and depyrogenation Day 3 AM ►Prepare risk based environmental assessments PM ►Understand the updates to ISO14644-1 and -2:2015 Module 8 – Solid Dosage Manufacture Principles and Practices (22 – 24 October 2018) – 3 day Course Aim: To provide an introduction to the GMP requirements for the formulation, scale up and optimization of Finished Solid Dose Forms and to develop a practical understanding of Process Mapping, Risk Analysis and Critical Control points, Validation requirements and Quality Plans as it applies to solid dose formulations.

Day 1 AM ►Granulation Technology and Control PM ► Blending and Milling Technology and Control Day 2 AM ►Encapsulation Technology and Control PM ►Compression Technology and Control Day 3 AM ►Coating Technology and Control PM ►Packaging Technology and Control

Module 4 - Good (Quality Control) Laboratory Practices (G(QC)LPs) (23 – 24 April 2018) – 2 day Course Aim: To facilitate the development of knowledge, and expertise in the regulations, quality standards and guidelines that govern the quality control of pharmaceuticals.

Day 1 AM ► Introduction to Good (Quality Control) Laboratory Practices (GLPs) PM ►Qualification and Calibration of Laboratory Equipment PM ►Analytical Method Validation Day 2 AM ►Biological assays Validation and Control PM ►Basic Statistics for Quality Control Laboratories

PM ►Pharmaceutical Sampling Plan & Pharmaceutical Stability Programs

FUNDAMENTAL COURSE OUTLINE

Back to back with Practical Stability

Study Application to Pharmaceuticals

to Pharmaceuticals (25 – 26 April

2018)

Recommended for: QA, QC

Recommended for: Engineering

Recommended for: QA, Warehousing, Distribution

With NEW CONTENT

Recommended for: QA and Production

Recommended for: Production and Engineering

Changed CONTENT

Practical Stability Study Application to Pharmaceuticals (25 – 26 April 2018) – 2 day Course

Aim: This course is designed to provide the quality professional with the key requirements for establishing and implementing a successful stability trial program. It will review the relevant ICH guidance documents and will include workshops to provide practical application of the key requirements for stability. It will develop techniques for planning new and on-going stability trials.

Day 1 AM ► ASEAN stability guidelines PM ► Preparation of stability protocol PM ► Bracketing and matrixing designs for new drug substances and products (ICH Q1D) Day 2 AM ► Evaluation of stability data (ICH Q1E) PM ► Registration applications in climatic zones III and IV (ICH Q1F)

PM ► FDA guideline on container/closure integrity

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Advanced Process Validation and Cleaning Validation (9 – 11 April 2018) – 3 day Course

Aim: To develop advanced understanding of Sterile and Non Sterile Process and Cleaning Validation in order to comply with contemporary regulatory expectations. Putting into perspective the interpretation of regulatory and industry guidance.

Day 1 AM ► Understanding ASEAN PV Guidance and SUPAC AM ► PIC/S Annex 15 and FDA Guidance on Process Validation

PM ► Ongoing re-validation Day 2 AM ► Process Performance Qualification AM ► Process capability analysis for process validation PM ► Developing a process validation rationale Day 3 AM ► The process equipment train and cleanability AM ► PDE a scientific approach to cleaning validation PM ► Introduction to CIP principles and validation

ADVANCED COURSE OUTLINE

With NEW CONTENT

Back with High

Demand Back to back with Module 5 - Good

(Quality Control) Laboratory Practices

(G(QC)LPs) (23 – 24 April 2018) Recommended for: QA, QC and Regulatory

Recommended for: QA, QC and Production

Pharmaceutical CAPA and Problem Solving (7 – 9 May 2018) – 3 day Course

Aim: To learn about how to use the CAPA system not only to satisfy regulatory requirements but also to implement a closed loop problem solving system to help minimise quality issues and improve compliance. To help identify regulatory requirements and expectations related to failure investigation, root cause analysis (RCA) and CAPA. A brief discussion on controls such as pharmacovigilance for drug products, FSCA and AE reporting for medical devices. Day 1 AM ► Defining CAPA PM ► Overview and Systematic application of the CAPA system as it applies to quality audits Day 2 AM ► Relationships between CAPA and risk assessment/management PM ► Risk assessment/management as it applies to audit observations Day 3 AM ► Application of CAPA to audit observation deficiencie PM ► How to perform Root Cause Analysis for a compliant CAPA

Recommended for: All Personnel

Risk Management in Pharmaceutical Operations (ICHQ9) (8 - 10 October 2018) – 3 day Course

Aim: To provide an introduction to the principles of risk management and its application in the pharmaceutical and related industries. To enable students to identify opportunities and apply risk principles within their GxP related operational areas.

Day 1 AM ► Principles of Risk Management and ICH Q9 PM ►Risk Management Techniques - FMEA, FTA, HACCP Day 2 AM ►Risk Management to Compliance and Quality Assurance Management PM ►Applying Risk Management in Compliance Day 3 AM ►Risk Management Principles in Validation Programs PM ►Applying Risk Management to Operations

Computer Systems for Regulated Environments/Data Integrity (25 – 27 June 2018) – 3 day Course

Aim: Computer Systems are an established and integral part of management in modern Life Science organisations. All users must ensure that their systems and software have been developed to best engineering practices in a quality assured and secure manner to comply with Regulatory Requirements and to be fit for Business Use. Data Integrity has become widely discussed as a global concern for the pharmaceutical industry. This section provides an introduction to develop a broad understanding of the scope of Data Integrity and how key principles may be applied in order to provide strategic elements necessary to ensure reliability and integrity of information and data throughout all aspects of a product’s lifecycle.

Day 1 AM ► Understand how computer systems are regulated in the local and global regulatory environment AM ► Understanding the controls necessary to demonstrate data integrity PM ► Computer Systems Selection and Vendor Qualification

Day 2 AM ► Developing a risk-based approach to CSV AM ► Best practices for validation test execution, documentation and error handling PM ► Understanding how the CSV process fits into the company’s Software Life Cycle (SLC), understand the types of, and elements of System Development Life Cycles (SDLC) and the use of GAMP 5

Day 3 AM ► Understanding of the key components and principles of a software quality assurance (SQA) program and auditor expectations.

PM ► Hands-on practice creating key validation deliverables, including requirements, test plan, test scripts and test summary PM ► Data Integrity:

➢ The definition of Data Integrity within a Quality Management System ➢ Governance of electronic data acquisition, manipulation and storage systems and Data Integrity for Good

Manufacturing Practice compliance

Module 9 – GxP and Quality Auditing Practices (26 – 27 November 2018) – 2 day Course

Aim: To provide an introduction to auditing principles and practices , and to develop a broad understanding of the requirements and techniques for planning, conducting and reporting quality audits applicable to manufacturing systems for drugs, biologics and devices.

Day 1 AM ►GxP audit schedule, managing regulatory audits in an effective manner, what to expect from GMP licensing audits PM ►The role of supplier audits for actives, excipients and components in Vendor management PM ► Four fundamental steps of auditing explained in detail, tips on how to manage & facilitate audits in a constructive manner Day 2 AM ► Utilisation of risk management in relation to prioritizing audits PM ► Auditing for data integrity

With NEW CONTENT

Recommended for: QA

Recommended for: QA

Recommended for: QA, QC and Engineering

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ADVANCED COURSE OUTLINE

METHODOLOGY: Lectures, workshops, case studies and group activities.

ASSESSMENT: A variety of assessment strategies will be used and may include assignments, classroom engagement, projects and presentations. Participants will be informed of the assessment method, date of assessment and percentage contribution at the start of the module.

Registration Fee per participant per module: (The fee includes course materials, lunch and refreshments)

MOPI Member – 3 day Course 30 days before commencement of course RM2,900.00

29 – 14 days before commencement of course RM3,100.00 13 – 7 days before commencement of course RM3,300,00

Non-MOPI Member – 3 day Course 30 days before commencement of course RM3,200.00

29 – 14 days before commencement of course RM3,400.00 13 – 7 days before commencement of course RM3,600.00

Foreign Participant – 3 day Course 30 days before commencement of course USD $1,300.00

29 – 14 days before commencement of course USD $1,500.00 13 – 7 days before commencement of course USD $1,700.00

Training Venue:

THE BOULEVARD St Giles Premier Hotel

Hotel Address | Mid Valley City |

Lingkaran Syed Putra | 59200 | Kuala Lumpur | Malaysia

Tel: +60.3.22958000 Website: www.StGiles-Hotels.com

BOOK YOUR SEAT NOW!!!

For further enquiries, please contact: Mike/Janet, MOPI

GLOBAL BUSINESS & CONVENTION CENTRE, MEZZANINE FLOOR, BLOCK A, NO. 8, JALAN 19/1, SECTION 19,

46300 PETALING JAYA, SELANGOER, WEST MALAYSIA Tel: 03-7931 9003 Fax: 03-7932 2730

E-mail: mike@mopi.org.my and admin@mopi.org.my www.mopi.org.my

TIME SCHEDULE: 9.00 am – 5.00 pm

8.30 am Registration 9.00 am AM Topic 10.15 am Tea Break 10.30 am AM Topic 12.15 pm Lunch 1.25 pm PM Topic 3.00 pm Tea Break 3.15 pm PM Topic 5.00 pm End

Registration

fee is

subjected to

6% GST

Optional Hotel accommodations: Cititel Mid Valley Tel: 603-2296 1188 Website: www.cititelmidvalley.com

Eastin Hotel, Petaling Jaya Tel: 603-7665 1111

Website: www.eastin.com

Crystal Crown Hotel, Petaling Jaya Tel : 603-7958 4422

Website: www.crystalcrown.com.my

Armada PJ Hotel Tel: 603-7954 6888

Website: www.armada.com.my

Registration Fee per participant per module: (The fee includes course materials, lunch and refreshments) MOPI Member – 2 day Course 30 days before commencement of course RM2,200.00 29 – 14 days before commencement of course RM2,400.00 13 – 7 days before commencement of course RM2,600,00 Non-MOPI Member – 2 day Course 30 days before commencement of course RM2,500.00 29 – 14 days before commencement of course RM2,700.00 13 – 7 days before commencement of course RM2,900.00

Foreign Participant – 2 day Course 30 days before commencement of course USD $900.00 29 – 14 days before commencement of course USD $1,100.00 13 – 7 days before commencement of course USD $1,300.00

ADMINISTRATION DETAILS:

Registration will be treated as confirmed only upon receipt of payment in full. CANCELLATIONS & TRANSFERS:

• If a registrant is unable to attend, a substitute candidate is welcome at no extra charge. Please provide the name and the title of the substitute participant at least 2 working days prior to the relevant course.

• Notice of cancellation by fax/email is required 14 working days prior to commencement of each module and refund less RM500 as administration charge will be made. However

a complete set of documentation will be sent to you.

• Regrettably, no refund can be made for cancellations received less than 10 working days prior to the commencement of each module. However a complete set of documentation will be sent to you.

• MOPI / SeerPharma reserves the right to cancel or reschedule the training modules. All efforts will be taken to inform participants of any change. MOPI /SeerPharma however will not be held liable for reimbursement of any claims or expenses should cancellation or rescheduling occur.

REGISTRATION FORM Subject to Administration details

Please register the following participant(s) for the above program. (To be completed in BLOCK LETTERS)

Enclosed cheque/bank draft No_______________for RM____________ being payment for _______ participant(s) made in favour of the

“Malaysian Organisation of Pharmaceutical Industries”.

Select a course accordingly:

Fundamental GMP Module Advanced GMP Module

Module 1 International Good Manufacturing Practices, Quality Management Systems and GMP for Pharmaceutical Operations 23 – 25 January 2018 (Tues - Thu) – 3 day Course

Advanced Process Validation and Cleaning Validation 9 – 11 April 2018 (Mon – Wed) – 3 day Course

Module 2 Validation Principles and Practices 5 – 7 February 2018 (Mon – Wed) – 3 day Course

Practical Stability Study Application to Pharmaceuticals 25 – 26 April 2018 (Wed – Thu) – 2 day Course

Behavourial GMP/ Good Documentation Practices/ Data Integrity 12 – 14 March 2018 (Mon – Wed) – 3 day Course

Pharmaceutical CAPA and Problem Solving 7 – 9 May 2018 (Mon – Wed) – 3 day Course

Module 3 Contamination Control 26 – 28 March 2018 (Mon – Wed) – 3 day Course

Computer Systems for Regulated Environments/Data Integrity 25 – 27 June (Mon – Wed) – 3 day Course

Module 4 Good Quality Control Laboratory Practices (G(QC)LPs) 23 – 24 April 2018 (Mon – Tue) – 2 day Course

Risk Management in Pharmaceutical Operations (ICH Q9) 8 – 10 October (Mon – Wed) – 3 day Course

Module 5 Compliance with GMP for the Pharmaceutical Engineer 23 – 25 July 2018 (Mon – Wed) – 3 day Course

Module 9 GxP and Quality Auditing Practices 26 - 27 November 2018 (Mon – Tue) – 2 day Course

Module 6 Good Distribution Practices (GDP) for the Regulated Industry 27 – 29 August 2018 (Mon – Wed) – 3 day Course

Module 7 Good Aseptic Practices & Sterile Products 24 – 26 September 2018 (Mon – Wed) – 3 day Course

Module 8 Solid Dosage Manufacture Principles and Practices 22 – 24 October 2018 (Mon – Wed) – 3 day Course

* * Dates and Instructors are subject to change depending on attendance

feedbacks and instructor availability. In case of a change, updated dates and

instructor profile will be advised to the organizer and the attendees prior to the

start of each course

Registration Submitted by:

Name _____________________________________________________

Designation ________________________________________________

E-mail ____________________________________________________

Company Stamp (with Address, Telephone & Fax Number)

Important Notice: Payment is required with registration and must be received 2 weeks prior to the start of the relevant module to guarantee your place. Walk-in participants will only be admitted on the basis of space availability at the course and with immediate full payment by banker’s cheque in favour of the

“Malaysian Organisation of Pharmaceutical Industries”.

Office Use Only

Registration Accepted on ………………….

Payment Accepted on ………………….….

2 Name____________________________________________________

Designation_______________________________________________ Email address _____________________________________________ Contact Number ___________________________________________

1 Name____________________________________________________

Designation_______________________________________________ Email address _____________________________________________

Contact Number ___________________________________________

MOPI Member Non-Member Foreign

Vegetarian Vegetarian

Registration Fee per participant per course: (The fee includes course materials, lunch and refreshments) MOPI Member – 3 day Course 30 days before commencement of course RM2,900.00 29 – 14 days before commencement of course RM3,100.00 13 – 7 days before commencement of course RM3,300,00 Non-MOPI Member – 3 day Course 30 days before commencement of course RM3,200.00 29 – 14 days before commencement of course RM3,400.00 13 – 7 days before commencement of course RM3,600.00

Foreign Participant – 3 day Course 30 days before commencement of course USD $1,300.00 29 – 14 days before commencement of course USD $1,500.00 13 – 7 days before commencement of course USD $1,700.00

Registration

fee is

subjected to

6% GST